Transduction optimization of AAV vectors for human gene therapy of glaucoma and their reversed cell entry characteristics

Gene Therapy, Published online: 14 October 2019; doi:10.1038/s41434-019-0105-4Transduction optimization of AAV vectors for human gene therapy of glaucoma and their reversed cell entry characteristics

https://www.nature.com/articles/s41434-019-0105-4

Source: Gene Therapy - October 13, 2019 Category: Genetics & Stem Cells Authors: Laura Rodriguez-Estevez Priyadarsini Asokan Teresa Borr ás Source Type: research

More News: Gene Therapy | Genetics | Glaucoma